Metabolic resuscitation in sepsis: a necessary step beyond the hemodynamic?
Autor(a) principal: | |
---|---|
Data de Publicação: | 2016 |
Outros Autores: | |
Tipo de documento: | Artigo |
Idioma: | por |
Título da fonte: | Repositório Institucional da UNIFESP |
dARK ID: | ark:/48912/001300000b702 |
Texto Completo: | http://dx.doi.org/10.21037/jtd.2016.05.37 https://repositorio.unifesp.br/handle/11600/57604 |
Resumo: | Despite the advances made in monitoring and treatment of sepsis and septic shock, many septic patients ultimately develop multiple organ dysfunction (MODS) and die, suggesting that other players are involved in the pathophysiology of this syndrome. Mitochondrial dysfunction occurs early in sepsis and has a central role in MODS development. MODS severity and recovery of mitochondrial function have been associated with survival. In recent clinical and experimental investigations, mitochondrion-target therapy for sepsis and septic shock has been suggested to reduce MODS severity and mortality. This intervention, which might be named "metabolic resuscitation", would lead to improved mitochondrial activity afforded by pharmacological and nutritional agents. Of particular interest in this therapeutic strategy is thiamine, a water-soluble vitamin that plays an essential role in cellular energy metabolism. Critical illness associated with hypermetabolic states may predispose susceptible individuals to the development of thiamine deficiency, which is not usually identified by clinicians as a source of lactic acidosis. The protective effects of thiamine on mitochondrial function may justify supplementation in septic patients at risk of deficiency. Perspectives of supplementation with other micronutrients (ascorbic acid, tocopherol, selenium and zinc) and potential metabolic resuscitators [coenzyme Q10 (CoQ10), cytochrome oxidase (CytOx), L-carnitine, melatonin] to target sepsis-induced mitochondrial dysfunction are also emerging. Metabolic resuscitation may probably be a safe and effective strategy in the treatment of septic shock in the future. However, until then, preliminary investigations should be replicated in further researches for confirmation. Better identification of groups of patients presumed to benefit clinically by a certain intervention directed to "mitochondrial resuscitation" are expected to increase driven by genomics and metabolomics. |
id |
UFSP_67560ea292da2923ff5cf06ec448b09d |
---|---|
oai_identifier_str |
oai:repositorio.unifesp.br/:11600/57604 |
network_acronym_str |
UFSP |
network_name_str |
Repositório Institucional da UNIFESP |
repository_id_str |
3465 |
spelling |
Metabolic resuscitation in sepsis: a necessary step beyond the hemodynamic?Mitochondriasepsismultiple organ failureoxidative stressthiamineseleniumDespite the advances made in monitoring and treatment of sepsis and septic shock, many septic patients ultimately develop multiple organ dysfunction (MODS) and die, suggesting that other players are involved in the pathophysiology of this syndrome. Mitochondrial dysfunction occurs early in sepsis and has a central role in MODS development. MODS severity and recovery of mitochondrial function have been associated with survival. In recent clinical and experimental investigations, mitochondrion-target therapy for sepsis and septic shock has been suggested to reduce MODS severity and mortality. This intervention, which might be named "metabolic resuscitation", would lead to improved mitochondrial activity afforded by pharmacological and nutritional agents. Of particular interest in this therapeutic strategy is thiamine, a water-soluble vitamin that plays an essential role in cellular energy metabolism. Critical illness associated with hypermetabolic states may predispose susceptible individuals to the development of thiamine deficiency, which is not usually identified by clinicians as a source of lactic acidosis. The protective effects of thiamine on mitochondrial function may justify supplementation in septic patients at risk of deficiency. Perspectives of supplementation with other micronutrients (ascorbic acid, tocopherol, selenium and zinc) and potential metabolic resuscitators [coenzyme Q10 (CoQ10), cytochrome oxidase (CytOx), L-carnitine, melatonin] to target sepsis-induced mitochondrial dysfunction are also emerging. Metabolic resuscitation may probably be a safe and effective strategy in the treatment of septic shock in the future. However, until then, preliminary investigations should be replicated in further researches for confirmation. Better identification of groups of patients presumed to benefit clinically by a certain intervention directed to "mitochondrial resuscitation" are expected to increase driven by genomics and metabolomics.Univ Fed Sao Paulo, Dept Pediat, Discipline Nutr & Metab, Rua Loefgreen 1647, Sao Paulo, BrazilUniv Fed Sao Paulo, Dept Pediat, Pediat Intens Care Unit, Sao Paulo, BrazilUniv Fed Sao Paulo, Dept Pediat, Discipline Nutr & Metab, Rua Loefgreen 1647, Sao Paulo, BrazilUniv Fed Sao Paulo, Dept Pediat, Pediat Intens Care Unit, Sao Paulo, BrazilWeb of SciencePioneer Bioscience Publ Co2020-08-14T13:44:20Z2020-08-14T13:44:20Z2016info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionE552-E557application/pdfhttp://dx.doi.org/10.21037/jtd.2016.05.37Journal Of Thoracic Disease. Hong Kong, v. 8, n. 7, p. E552-E557, 2016.10.21037/jtd.2016.05.37WOS000385021800016.pdf2072-1439https://repositorio.unifesp.br/handle/11600/57604WOS:000385021800016ark:/48912/001300000b702porJournal Of Thoracic DiseaseHong Konginfo:eu-repo/semantics/openAccessLeite, Heitor Pons [UNIFESP]Peixoto de Lima, Lucio Flavio [UNIFESP]reponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-08-01T09:04:19Zoai:repositorio.unifesp.br/:11600/57604Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-12-11T20:08:40.232473Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false |
dc.title.none.fl_str_mv |
Metabolic resuscitation in sepsis: a necessary step beyond the hemodynamic? |
title |
Metabolic resuscitation in sepsis: a necessary step beyond the hemodynamic? |
spellingShingle |
Metabolic resuscitation in sepsis: a necessary step beyond the hemodynamic? Leite, Heitor Pons [UNIFESP] Mitochondria sepsis multiple organ failure oxidative stress thiamine selenium |
title_short |
Metabolic resuscitation in sepsis: a necessary step beyond the hemodynamic? |
title_full |
Metabolic resuscitation in sepsis: a necessary step beyond the hemodynamic? |
title_fullStr |
Metabolic resuscitation in sepsis: a necessary step beyond the hemodynamic? |
title_full_unstemmed |
Metabolic resuscitation in sepsis: a necessary step beyond the hemodynamic? |
title_sort |
Metabolic resuscitation in sepsis: a necessary step beyond the hemodynamic? |
author |
Leite, Heitor Pons [UNIFESP] |
author_facet |
Leite, Heitor Pons [UNIFESP] Peixoto de Lima, Lucio Flavio [UNIFESP] |
author_role |
author |
author2 |
Peixoto de Lima, Lucio Flavio [UNIFESP] |
author2_role |
author |
dc.contributor.author.fl_str_mv |
Leite, Heitor Pons [UNIFESP] Peixoto de Lima, Lucio Flavio [UNIFESP] |
dc.subject.por.fl_str_mv |
Mitochondria sepsis multiple organ failure oxidative stress thiamine selenium |
topic |
Mitochondria sepsis multiple organ failure oxidative stress thiamine selenium |
description |
Despite the advances made in monitoring and treatment of sepsis and septic shock, many septic patients ultimately develop multiple organ dysfunction (MODS) and die, suggesting that other players are involved in the pathophysiology of this syndrome. Mitochondrial dysfunction occurs early in sepsis and has a central role in MODS development. MODS severity and recovery of mitochondrial function have been associated with survival. In recent clinical and experimental investigations, mitochondrion-target therapy for sepsis and septic shock has been suggested to reduce MODS severity and mortality. This intervention, which might be named "metabolic resuscitation", would lead to improved mitochondrial activity afforded by pharmacological and nutritional agents. Of particular interest in this therapeutic strategy is thiamine, a water-soluble vitamin that plays an essential role in cellular energy metabolism. Critical illness associated with hypermetabolic states may predispose susceptible individuals to the development of thiamine deficiency, which is not usually identified by clinicians as a source of lactic acidosis. The protective effects of thiamine on mitochondrial function may justify supplementation in septic patients at risk of deficiency. Perspectives of supplementation with other micronutrients (ascorbic acid, tocopherol, selenium and zinc) and potential metabolic resuscitators [coenzyme Q10 (CoQ10), cytochrome oxidase (CytOx), L-carnitine, melatonin] to target sepsis-induced mitochondrial dysfunction are also emerging. Metabolic resuscitation may probably be a safe and effective strategy in the treatment of septic shock in the future. However, until then, preliminary investigations should be replicated in further researches for confirmation. Better identification of groups of patients presumed to benefit clinically by a certain intervention directed to "mitochondrial resuscitation" are expected to increase driven by genomics and metabolomics. |
publishDate |
2016 |
dc.date.none.fl_str_mv |
2016 2020-08-14T13:44:20Z 2020-08-14T13:44:20Z |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.21037/jtd.2016.05.37 Journal Of Thoracic Disease. Hong Kong, v. 8, n. 7, p. E552-E557, 2016. 10.21037/jtd.2016.05.37 WOS000385021800016.pdf 2072-1439 https://repositorio.unifesp.br/handle/11600/57604 WOS:000385021800016 |
dc.identifier.dark.fl_str_mv |
ark:/48912/001300000b702 |
url |
http://dx.doi.org/10.21037/jtd.2016.05.37 https://repositorio.unifesp.br/handle/11600/57604 |
identifier_str_mv |
Journal Of Thoracic Disease. Hong Kong, v. 8, n. 7, p. E552-E557, 2016. 10.21037/jtd.2016.05.37 WOS000385021800016.pdf 2072-1439 WOS:000385021800016 ark:/48912/001300000b702 |
dc.language.iso.fl_str_mv |
por |
language |
por |
dc.relation.none.fl_str_mv |
Journal Of Thoracic Disease |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
E552-E557 application/pdf |
dc.coverage.none.fl_str_mv |
Hong Kong |
dc.publisher.none.fl_str_mv |
Pioneer Bioscience Publ Co |
publisher.none.fl_str_mv |
Pioneer Bioscience Publ Co |
dc.source.none.fl_str_mv |
reponame:Repositório Institucional da UNIFESP instname:Universidade Federal de São Paulo (UNIFESP) instacron:UNIFESP |
instname_str |
Universidade Federal de São Paulo (UNIFESP) |
instacron_str |
UNIFESP |
institution |
UNIFESP |
reponame_str |
Repositório Institucional da UNIFESP |
collection |
Repositório Institucional da UNIFESP |
repository.name.fl_str_mv |
Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP) |
repository.mail.fl_str_mv |
biblioteca.csp@unifesp.br |
_version_ |
1818602436529487872 |